lmod3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3878822	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 69,158,226-69,171,557 , GRCh38.p12 chr3: 69,109,075-69,122,406	LMOD3
nsv3916461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960	LMOD3, LOC105377171, 323 more genes
nsv3922768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938	LMOD3, RNU6-557P, 147 more genes
nsv6290933	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 59,332,508-70,686,155 , GRCh38.p12 chr3: 59,346,782-70,637,004	LMOD3, NDUFB4P1, 110 more genes
nsv3883532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 66,133,719-75,076,440 , GRCh38.p12 chr3: 66,148,044-75,027,289	LMOD3, PSMD12P1, 93 more genes
nsv3917061	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 68,940,430-75,092,800 , GRCh37.p13 chr3: 68,857,740-75,010,110 , GRCh38.p12 chr3: 68,808,589-74,960,959	LMOD3, RYBP, 69 more genes
nsv3920193	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 67,441,430-73,463,152 , NCBI36 chr3: 67,524,120-73,545,842 , GRCh38 chr3: 67,391,006-73,414,001	LMOD3, RNPC3P1, 65 more genes
nsv5564432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267	LMOD3, CCDC137P1, 39 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	LMOD3, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	LMOD3, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	LMOD3, RPL23AP49, 2875 more genes
nsv3913280	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr3: 68,460,820-76,896,160 , GRCh37 chr3: 68,378,130-76,813,470 , GRCh38 chr3: 68,328,980-76,764,319	LMOD3, AKR1B1P2, 105 more genes
nsv3875054	copy number variation	1	nstd102	human	not provided	GRCh37 chr3: 68,461,188-69,158,250 , GRCh38.p12 chr3: 68,412,038-69,109,099	LMOD3, RPLP0P8, 10 more genes
nsv6290797	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 68,968,872-70,829,637 , GRCh38.p12 chr3: 68,919,721-70,780,486	LMOD3, UBA3, 17 more genes
nsv4453115	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 68,831,471-69,535,890 , GRCh38.p12 chr3: 68,782,320-69,486,739	LMOD3, ARL6IP5, 8 more genes

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